The First School of Clinical Medicine, Lanzhou University, Lanzhou, Gansu, China.
Department of Anesthesiology, Shandong Cancer Hospital and Institute Affiliated to Shandong First Medical University, Shandong Academy of Medical Science, Jinan, Shandong, China.
BMC Anesthesiol. 2024 May 8;24(1):172. doi: 10.1186/s12871-024-02524-7.
Low immune function after laparoscopic total gastrectomy puts patients at risk of infection-related complications. Low-dose naloxone (LDN) can improve the prognosis of patients suffering from chronic inflammatory diseases or autoimmune diseases. The use of LDN during perioperative procedures may reduce perioperative complications. The purpose of this study was to examine the effects of LDN on endogenous immune function in gastric cancer patients and its specific mechanisms through a randomized controlled trial.
Fifty-five patients who underwent laparoscopic-assisted total gastrectomy were randomly assigned to either a naloxone group (n = 23) or a nonnaloxone group (n = 22). Patients in the naloxone group received 0.05 µg/kg-1.hnaloxone from 3 days before surgery to 5 days after surgery via a patient-controlled intravenous injection (PCIA) pump, and patients in the nonnaloxone group did not receive special treatment. The primary outcomes were the rates of postoperative complications and immune function assessed by NK cell, CD3 T cell, CD4 T cell, CD8 T cell, WBC count, neutrophil percentage, and IL-6 and calcitonin levels. The secondary outcomes were the expression levels of TLR4 (Toll-like receptor), IL-6 and TNF-α in gastric cancer tissue.
Compared with the nonnaloxone group, the naloxone group exhibited a lower incidence of infection (in the incision, abdomen, and lungs) (P < 0.05). The numbers of NK cells and CD8 T cells in the naloxone group were significantly greater than those in the nonnaloxone group at 24 h after surgery (P < 0.05) and at 96 h after surgery (P < 0.05). Compared with those in the nonnaloxone group, the CD3 T-cell (P < 0.05) and CD4 T-cell (P < 0.01) counts were significantly lower in the naloxone group 24 h after surgery. At 24 h and 96 h after surgery, the WBC count (P < 0.05) and neutrophil percentage (P < 0.05) were significantly greater in the nonnaloxone group. The levels of IL-6 (P < 0.05) and calcitonin in the nonnaloxone group were significantly greater at 24 h after surgery. At 24 h following surgery, the nonnaloxone group had significantly greater levels of IL-6 (P < 0.05) and calcitonin than did the naloxone group. Compared with those in the naloxone group, the expression levels of TLR4 (P < 0.05) in gastric cancer tissue in the naloxone group were greater; however, the expression levels of IL-6 (P < 0.01) and TNF-α (P < 0.01) in the naloxone group were greater than those in the nonnaloxone group.
Laparoscopic total gastrectomy patients can benefit from 0.05 ug/kg. h naloxone by reducing their risk of infection. It is possible that LDN alters the number of cells in lymphocyte subpopulations, such as NK cells, CD3 T cells, and CD4T cells, and the CD4/CD8 T-cell ratio or alters TLR4 receptor expression in immune cells, thereby altering immune cell activity.
The trial was registered at the Chinese Clinical Trial Registry on 24/11/2023 (ChiCTR2300077948).
腹腔镜全胃切除术后患者的免疫功能低下,存在感染相关并发症的风险。小剂量纳洛酮(LDN)可改善慢性炎症性疾病或自身免疫性疾病患者的预后。围手术期使用 LDN 可能会减少围手术期并发症。本研究旨在通过随机对照试验,探讨 LDN 对胃癌患者内源性免疫功能的影响及其具体机制。
55 例行腹腔镜辅助全胃切除术的患者被随机分配到纳洛酮组(n=23)或非纳洛酮组(n=22)。纳洛酮组患者从术前 3 天至术后 5 天通过患者自控静脉注射(PCIA)泵接受 0.05μg/kg-1.h 纳洛酮,而非纳洛酮组患者未接受特殊治疗。主要结局为术后并发症发生率和 NK 细胞、CD3 T 细胞、CD4 T 细胞、CD8 T 细胞、白细胞计数、中性粒细胞百分比、IL-6 和降钙素水平评估的免疫功能。次要结局为胃癌组织中 TLR4(Toll 样受体)、IL-6 和 TNF-α 的表达水平。
与非纳洛酮组相比,纳洛酮组感染(切口、腹部和肺部)发生率较低(P<0.05)。术后 24 小时和 96 小时,纳洛酮组 NK 细胞和 CD8 T 细胞数量明显多于非纳洛酮组(P<0.05)。与非纳洛酮组相比,纳洛酮组术后 24 小时 CD3 T 细胞(P<0.05)和 CD4 T 细胞(P<0.01)计数明显较低。术后 24 小时和 96 小时,非纳洛酮组白细胞计数(P<0.05)和中性粒细胞百分比(P<0.05)明显较高。术后 24 小时,非纳洛酮组 IL-6(P<0.05)和降钙素水平明显较高。术后 24 小时,非纳洛酮组 IL-6(P<0.05)和降钙素水平明显高于纳洛酮组。与纳洛酮组相比,纳洛酮组胃癌组织中 TLR4 表达水平(P<0.05)较高;然而,纳洛酮组 IL-6(P<0.01)和 TNF-α(P<0.01)表达水平高于非纳洛酮组。
腹腔镜全胃切除术患者可受益于 0.05μg/kg.h 纳洛酮,降低感染风险。LDN 可能通过改变 NK 细胞、CD3 T 细胞和 CD4 T 细胞等淋巴细胞亚群的细胞数量或改变免疫细胞中 TLR4 受体的表达,从而改变免疫细胞的活性,从而改变免疫细胞的数量。
该试验于 2023 年 11 月 24 日在中国临床试验注册中心注册(ChiCTR2300077948)。